SNP Detail For rs17515225
1.Mapping Information
Human SNP ID rs17515225
Human chromosome chr2
Human SNP position 140788186
Pig chromosome chr15
Pig SNP position 12334053
2.Annotation Information
PubMed ID25628336
JournalHum Mol Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/25628336
StudyGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.
Disease/TraitMotion sickness
Initial sample80,494 European ancestry individuals
Replication sampleNA
Region2q22.1
Chromosome idchr2
Chromosome position140788186
Reported geneLRP1B
Mapped geneLRP1B
Upstream gene id
Downstream gene id
SNP gene ids53353
Upstream gene distance
Downstream gene distance
SNP risk allelers17515225-T
SNPsrs17515225
Merged0
SNP id current17515225
Contextintron_variant
Intergenic0
Allele frequency0.445
P value0.000000003
Pvalue mlog8.52287874528033
P value text
Or beta0.032
%95 Ci[0.021-0.042] unit increase
PlatformIllumina [7428049] (imputed)
CNVN
Mapped traitmotion sickness
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0006928
Study accessionGCST002759